PDE4 inhibitors as new anti-inflammatory drugs: Effects on cell trafficking and cell adhesion molecules expression

被引:91
作者
Sanz, MJ
Cortijo, J
Morcillo, EJ
机构
[1] Univ Valencia, Fac Med, Dept Pharmacol, E-46010 Valencia, Spain
[2] Univ Gen Hosp Consortium, Res Fdn, Valencia, Spain
关键词
phosphodiesterase; 4; inhibitors; cell adhesion molecules; cytokines; chemokines; inflammation;
D O I
10.1016/j.pharmthera.2004.12.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Phosphodiesterase 4 (PDE4) is a major cyclic AMP-hydrolyzing enzyme in inflammatory and immunomodulatory cells. The wide range of inflammatory mechanisms under control by PDE4 points to this isoenzyme as an attractive target for new anti-inflammatory drugs. Selective inhibitors of PDE4 have demonstrated a broad spectrum of anti-inflammatory activities including the inhibition of cellular trafficking and microvascular leakage, cytokine and chemokine release from inflammatory cells, reactive oxygen species production, and cell adhesion molecule expression in a variety of in vitro and in vivo experimental models. The initially detected side effects, mainly nausea and emesis, appear at least partially overcome by the 'second generation' PDE4 inhibitors, some of which like roflumilast and cilomilast are in the later stages of clinical development for treatment of chronic obstructive pulmonary disease. These new drugs may also offer opportunities for treatment of other inflammatory diseases. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:269 / 297
页数:29
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